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Operátor procesu v biofarmaceutickej výrobe

AdeccoID:18273

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Miesto výkonu
Dánsko | Frederiksberg
Nástup do práce
dohodou
Ponúkaná mzda
dohodou
Druh pracovného pomeru
plný úväzok
Popis pracovnej ponuky:

For the Drug Substance Manufacturing Unit in Hillerød, Fujifilm Diosynth Biotechnologies is looking for Manufacturing Associates (Process Operators) to support the expansion project.

 

FUJIFILM Diosynth Biotechnologies is currently expanding its capacity to support the large-scale production by adding 14 x 20,000L bioreactors and three downstream processing lines in Hillerød. The additional production capacity will make the facility the largest end-to-end Contract Development and Manufacturing Organization (CDMO) in Europe, offering a total of 20 x 20,000L bioreactors for drug substance production complemented by comprehensive drug product and finished goods services.

This is an excellent opportunity to join our company at a pivotal time of growth and be part of an exciting journey.

 

We are currently looking for candidates to support the expansion with the Commissioning Readiness of all Systems, to support Equipment Start-up and IOQ Testing. This is an excellent opportunity to get extensive knowledge on the manufacturing equipment before we go into production in 2024. The expansion project is set to end in approx. April 2024.

 

When the project is finished you will automatically be offered a job opportunity in our new Drug Substance Manufacturing department covering – respectively – Upstream & Downstream. The two departments cover different steps in the biopharmaceutical production such as Media Preparation, CIP & SIP of equipment, growth of cell cultures, and purification via multiple column steps.

 

During the first period of the project working hours will be mon-fri 08-16. But as we move further in to the project and into the testing phase we will go into shift work.

Tasks

  • Support and review design deliverables incl. drawings, data sheets, specifications and engineering lists.
  • Perform field walk-downs and participate actively in weekly/monthly meetings and ensure timely updates
  • Ensure timely approval of Final reports and create training documents
  • Equipment testing
  • Trouble shooting
Dátum platnosti do:
08.06.2023
Voľné pracovné miesta:
1
ISCO:
farmaceutický laborant v technológii prípravy liekov
NACE:
výroba základných farmaceutických výrobkov a farmaceutických prípravkov
Požiadavky:

We imagine that you:

  • Have education as industrial operator, process technologist process operators or similar, preferable with experience from a similar pharmaceutical production company or similar regulated businesses
  • Are a Life Sciences Graduate who have recently finalized your Bachelor or master’s degree relevant for Biologics Manufacturing and are keen on starting your career in a manufacturing and international environment where things move fast
  • Experience with cGMP and/or SOPs
  • Have an interest in working with numbers, math’s and IT tools.

It is a plus if you have experience or knowledge of chromatography and filtration processes.

You will get the opportunity to customize your development plan in agreement with your manager based on your wishes and qualifications.

Personal skills

We are hiring for attitude, so we are looking for people who have a lot of drive and interest with working under GMP.

You are:

  • quality-oriented and thorough
  • Proactive and organized
  • responsible and able to take ownership of tasks.
  • a good team player who thrives on setting a good example
  • keen on learning new things, and the first period will of course include thorough training.
Požadované vzdelanie:
vysoká škola
Jazyk a úroveň ovládania:
anglický - B2 Samostatný používateľ
Pozícia vhodná pre absolventa:
áno
Trvanie pracovného pomeru:
doba neurčitá
Doplňujúce informácie:

FUJIFILM Diosynth Biotechnologies is currently expanding its capacity to support the large-scale production by adding 14 x 20,000L bioreactors and three downstream processing lines in Hillerød. The additional production capacity will make the facility the largest end-to-end Contract Development and Manufacturing Organization (CDMO) in Europe, offering a total of 20 x 20,000L bioreactors for drug substance production complemented by comprehensive drug product and finished goods services.

Ponuka agentúry:
áno
Kontakt:

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EURES poradca: Mgr. Ferdinand Bolibruch
Email: ferdinand.bolibruch@upsvr.gov.sk
Telefón: 043/2445303